CLASS II Food recall · Reported 22 Jan 2020 · FDA Enforcement Report
Tobago Keys Coral Ridge Seafood Dipping Sauce recalled
Endorphin Farms is recalling Tobago Keys Coral Ridge Seafood Dipping Sauce and Peruvian Gold Grilling Sauce, distributed in Florida, North Carolina. The recall was initiated on 21 Nov 2019 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0560-2020
- FDA event ID
- 84606
- Recalling firm
- Endorphin Farms, Saint Augustine, FL
- Brand
- Tobago Keys
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 21 Nov 2019
- FDA classified
- 24 Jan 2020
- Reported
- 22 Jan 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Undeclared Fish & Shellfish
- Product category
- Sauces & Condiments
Timeline
| 21 Nov 2019 | Recall initiated by company | |
| 22 Jan 2020 | Published in enforcement report | +62 days |
| 24 Jan 2020 | Classified by FDA | +2 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Product labels were applied to wrong product resulting in an undeclared fish allergen.
Product as listed by the FDA
Tobago Keys brand Coral Ridge Seafood Dipping Sauce 12 FL.OZ. (355 ml) and Peruvian Gold Grilling Sauce 12 FL.OZ (355 ml)
Where it was distributed
Product was distributed to 4 consignees, 3 in Florida and one in North Carolina.
Questions about this recall
Why was it recalled?
Product labels were applied to wrong product resulting in an undeclared fish allergen.
Which lots are affected?
TTPGOCT092021EF
Where was it sold?
Product was distributed to 4 consignees, 3 in Florida and one in North Carolina.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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